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— US FDA Reviewer for 10 years, conducted primary and critical reviews of numerous IND and NDA applications for both small molecules and biologics
— VP of Drug Development and Regulatory Affairs of BeiGene, CEO of BL Pharma, and CTO of JOINN Laboratories
— In the past 20+ years, he devoted into new drug R&D in different stakeholders from FDA, CRO to biotech companies. He gained rich experience by leading global new drug development, non-clinical and clinical trial designs, GLP, GCP regulations, molecule selection, developability assessment, and project risk management
— Committee member of the Chinese Pharmaceutical Association, Council member of AAALAC, member of editorial board of Chinese Journal of New Drugs, Progress in Pharmaceutical Sciences and DIA advisory committee
— Post-doc research in National Institutes of Health from 1996 to 1998, Ph.D. degree in Toxicology from New York University in 1996 and medical degree from Beijing Medical College in 1984
— Program Lead of China “Key Innovative Drug Development Program”
— Bachelor in Clinical medicine, Peking University School of Medicine; Master's degree, the University of Toledo; Ph.D. in Biological Engineering, MIT
— Worked for Celgene, Bristol Myers Squibb and Astrazeneca, 20+ years leadership experience in global clinical operations
— Bachelor in Medicine, Sun Yat-sen University; Master in Accountancy, University of South Carolina
— Member of AICPA, worked for United Technologies and Anthem, 20+ years as global healthcare financial management executive in US MNC, health insurance company and big 4 audit firms
— Master in Pharmacognosy, Peking University School of Medicine
— Worked as deputy director of product design center in Taiji Group in Beijing, responsible for product registration and regulatory communication, 15 years' experience in drug registration
— Ph.D. in Biology, Center for Excellence in Molecular Cell Science, CAS
— Worked for GlaxoSmithKline and the Institute of Health Sciences, experienced in biomarker validation and translational medicine
— Ph.D. in Organic Chemistry, Chinese Academy of Sciences; Post-doc, The Ohio State University; Post-doc, University of California, Riverside
— Worked for Pharmaron, Wuxi AppTec, Acme Bioscience, and Berlex Biosciences, 20 years’ experience in drug discovery and development in medicinal chemistry
— Productive research results: 2 clinical candidate drugs 10 pre-clinical candidate drugs
— Bachelor in Clinical Medicine, Peking University School of Medicine; Ph.D. & Master in Biostatistics, University of Minnesota
— Worked for Bristol Myers Squibb, was in charge of Nivolumab (OPDIVO®) NSCLC Project Analytics
— Bachelor in Pharmacy, Monash University
— Worked for Celgene, PRA Health Sciences, PPD and Quintiles, 20 years' experience in global clinical research
— Master in Clinical Medicine, West China Hospital, Sichuan University
— Worked for BeiGene, Biotech Pharma and Tong-yang Pharmaceuticals, 17 years' clinical research experience
— Bachelor in Finance, Suzhou University
— Previous experience in WuXi AppTec, JOINN Laboratories and BL Pharma, 17 years operation management experience
— Ph.D. in Psychology, East China Normal University
— Previous experience in ciic Consulting, Luolai Home Textile and SAIC-GM, 18 years' experience in human resource management
— Bachelor in Clinical medicine, Peking University School of Medicine; Master’s degree, the University of Toledo; Ph.D. in Biological Engineering, MIT
— Worked for Celgene, Bristol Myers Squibb and Astrazeneca, 20+ years leadership experience in global clinical operations
— Bachelor in Medicine, Sun Yat-sen University; Master in Accountancy, University of South Carolina
— Member of AICPA, worked for United Technologies and Anthem, 20+ years as global healthcare financial management executive in US MNC, health insurance company and big 4 audit firms
— Master in Pharmacognosy, Peking University School of Medicine
— Worked as deputy director of product design center in Taiji Group in Beijing, responsible for product registration and regulatory communication, 15 years' experience in drug registration
— Ph.D. in Biology, Center for Excellence in Molecular Cell Science, CAS
— Worked for GlaxoSmithKline and the Institute of Health Sciences, experienced in biomarker validation and translational medicine
— Ph.D. in Organic Chemistry, Chinese Academy of Sciences; Post-doc, The Ohio State University; Post-doc, University of California, Riverside
— Worked for Pharmaron, Wuxi AppTec, Acme Bioscience, and Berlex Biosciences, 20 years' experience in drug discovery and development in medicinal chemistry
— Productive research results: 2 clinical candidate drugs 10 pre-clinical candidate drugs
— Bachelor in Clinical Medicine, Peking University School of Medicine; Ph.D. & Master in Biostatistics, University of Minnesota
— Worked for Bristol Myers Squibb, was in charge of Nivolumab (OPDIVO®) NSCLC Project Analytics
— Bachelor in Pharmacy, Monash University
— Worked for Celgene, PRA Health Sciences, PPD and Quintiles, 20 years' experience in global clinical research
— Master in Clinical Medicine, West China Hospital, Sichuan University
— Worked for BeiGene, Biotech Pharma and Tong-yang Pharmaceuticals, 17 years' clinical research experience
— Bachelor in Finance, Suzhou University
— Previous experience in WuXi AppTec, JOINN Laboratories and BL Pharma, 17 years operation management experience
Ph.D. in Psychology, East China Normal University
Previous experience in ciic Consulting, Luolai Home Textile and SAIC-GM, 18 years’ experience in human resource management